Your tasks
- Overall responsibility for the areas of engineering, maintenance, and IT
- Ensuring GMP-compliant planning, implementation, and maintenance of equipment, systems, and infrastructure
- Leading and developing a small interdisciplinary team
- Responsibility for qualification/validation (IQ/OQ/PQ) of equipment and IT systems
- Management of capital projects (CAPEX), including budget responsibility
- Ensuring IT compliance (e.g., CSV, data integrity, 21 CFR Part 11)
- Collaboration with QA, production, and external partners
- Preparation for and support during audits and inspections
Your profile
- Bachelor’s degree or technical degree with professional experience in pharmaceutical engineering, mechatronics, or a comparable qualification
- Professional experience in the technical support of pharmaceutical or biotechnology production equipment and facilities
- Experience in equipment and facility qualification
- In-depth knowledge of GMP regulations, qualification /validation, and IT systems in regulated environments
- A hands-on and independent approach to work in a dynamic environment
- Strong communication skills and the ability to work well in a team
- Good knowledge of MS Office
- Fluent German and very good English skills
Our Offering
- A permanent employment contract
- A pleasant working atmosphere in a dynamic team
- A challenging role with a high degree of autonomy
- Professional development opportunities
- JOBRAD
- Regular company events
- A family-friendly and expanding company
Your new employer
Intavis Peptide Services is a small but rapidly-growing biotech company that specializes in producing customized peptides for both laboratory and clinical research. At Intavis Peptide Services, we believe in the power of peptides to create new therapies for currently uncureable diseases.
Intavis develops and manufactures custom peptides for laboratory, discovery, and preclinical research. As part of our continued growth, we are expanding our production capabilities for Research and Advanced Grade products and are looking for new colleagues to join our team.
Applications via email to hr@intavispeptides.com
Intavis Peptide Services
Founded in the late 1990s Intavis Peptide Services (IPS) has around 30 years of experience in peptide synthesis. As a part of the Intavis Instruments corporation we initially synthesized peptides to validate analytical instruments. However, when the scientific and medical community realized the great potential of peptide drugs, such as Insulin and many more peptide-based blockbusters, Intavis expanded their custom peptide synthesis division. Until today, IPS has contributed to many research projects and partnered with global companies (link). IPS provides comprehensive service around customized peptide synthesis – from project inception to final peptide-based medicinal product (link). Indeed, our products are also used in vaccine development and personalized cancer therapy.
Intavis Peptide Services blends hands-on experience, scientific knowledge and dedicated employees to a unique service offering for their customers. Our seasoned leadership team has decades of experience in the biotech and life science space and our partners support us with their expertise and network (link). Our reliability, effectiveness and customer focus earned us an excellent reputation in the custom peptide synthesis space.
Order your peptides
Click order and a form will pop-up so you can enter your sequence directly. Alternatively upload a document listing your peptides or conjugates.